@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_head {
  this: np:hasAssertion dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_assertion ;
    np:hasProvenance dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_provenance ;
    np:hasPublicationInfo dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_assertion a np:Assertion .
  dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_provenance a np:Provenance .
  dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  lld:C0242583 a ncit:C7057 .
  dgn-gda:DGNfd234c3aebf84e7affd285adb0b008c4 sio:SIO_000628 miriam-gene:4397 , lld:C0242583 ;
    a sio:SIO_001121 .
}
dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_provenance {
  dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_assertion dcterms:description "[Because of the central role the class II MHC molecules play in immune system function, it is not surprising that the lack of expression of these molecules results in a severe combined immunodeficiency disorder (called bare lymphocyte syndrome) and that the aberrant expression of the molecules is frequently observed in the target organs of various autoimmune disorders (e.g., multiple sclerosis and rheumatoid arthritis).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:7589984 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP873557.RAYPsdW_3MoqdmzihplQslDRArfIp2NTn2llD2d_tQeRU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:54+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}